Canonical Allele Identifier: CA2397958078
Gene: SMARCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23787024A= , CM000684.2:g.23787024A= GRCh38
NC_000022.10:g.24129211A= , CM000684.1:g.24129211A= GRCh37
NC_000022.9:g.22459211A= NCBI36
NG_009303.1:g.5062A= , LRG_520:g.5062A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263121.12:c.-146A= ENSP00000263121.8:n.-146A=
ENST00000344921.11:c.-146A= ENSP00000340883.6:n.-146A=
ENST00000407082.4:c.-146A= ENSP00000385226.4:n.-146A=
ENST00000407422.8:c.-146A= ENSP00000383984.3:n.-146A=
ENST00000491967.2:n.45A=
ENST00000644036.2:c.-146A= MANE Select ENSP00000494049.2:n.-146A=
ENST00000644619.1:c.-146A= ENSP00000494695.1:n.-146A=
ENST00000646421.1:n.47A=
ENST00000647057.1:c.-146A= ENSP00000494757.1:n.-146A=
ENST00000263121.11:c.-146A= ENSP00000263121.7:n.-146A=
ENST00000344921.10:c.-146A= ENSP00000340883.6:n.-146A=
ENST00000407082.3:c.-146A= ENSP00000385226.3:n.-146A=
ENST00000407422.7:c.-146A= ENSP00000383984.3:n.-146A=
ENST00000417137.5:c.-146A= ENSP00000388489.1:n.-146A=
NM_001007468.1:c.-146A= NP_001007469.1:n.-146A=
NM_003073.3:c.-146A= , LRG_520t1:c.-146A= NP_003064.2:n.-146A=
XM_011530345.1:c.-146A= XP_011528647.1:n.-146A=
XM_011530346.1:c.-146A= XP_011528648.1:n.-146A=
NM_001007468.2:c.-146A= NP_001007469.1:n.-146A=
NM_001317946.1:c.-146A= NP_001304875.1:n.-146A=
NM_001362877.1:c.-146A= NP_001349806.1:n.-146A=
NM_003073.4:c.-146A= NP_003064.2:n.-146A=
NM_001007468.3:c.-146A= NP_001007469.1:n.-146A=
NM_001317946.2:c.-146A= NP_001304875.1:n.-146A=
NM_001362877.2:c.-146A= NP_001349806.1:n.-146A=
NM_003073.5:c.-146A= MANE Select NP_003064.2:n.-146A=